Respiratory system with humidifier and conformable reservoir

ABSTRACT

A humidifier for humidifying a flow of air to be delivered to a patient includes a base unit having at least one wall defining a receiving space. The base unit also includes a variable volume reservoir configured to hold a body of water and receive the flow of air to humidify the flow of air for delivery to the patient. The receiving space is configured to receive the variable volume reservoir and the variable volume reservoir is conformable to a shape of the receiving space. The humidifier further includes a heater for heating the body of water.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a non-provisional of U.S. Application No.62/237,206, filed Oct. 5, 2015, the entire contents of whichincorporated herein by reference.

1 BACKGROUND OF THE TECHNOLOGY

1.1 Field of the Technology

The present technology relates to one or more of the detection,diagnosis, treatment, prevention and amelioration of respiratory-relateddisorders. The present technology also relates to medical devices orapparatus, and their use.

1.2 Description of the Related Art

1.2.1 Human Respiratory System and its Disorders

The respiratory system of the body facilitates gas exchange. The noseand mouth form the entrance to the airways of a patient.

A range of respiratory disorders exist. Examples of respiratorydisorders may include (and/or may be related to) Obstructive Sleep Apnea(OSA), Cheyne-Stokes Respiration (CSR), Respiratory Insufficiency,Obesity Hyperventilation Syndrome (OHS), Chronic Obstructive PulmonaryDisease (COPD), Neuromuscular Disease (NMD) and Chest wall disorders.Certain disorders may be characterised by particular events, e.g.apneas, hypopneas, and hyperpneas.

A range of therapies have been used to treat or ameliorate suchconditions. Furthermore, otherwise healthy individuals may takeadvantage of such therapies to prevent respiratory disorders fromarising. However, these have a number of shortcomings.

1.2.2 Therapy

Examples of respiratory therapies include: (i) Continuous PositiveAirway Pressure (CPAP) therapy, which has been used to treat ObstructiveSleep Apnea (OSA); (ii) Non-invasive ventilation (NIV), which providesventilatory support to a patient through the upper airways to assist thepatient breathing and/or maintain adequate oxygen levels in the body bydoing some or all of the work of breathing via a non-invasive patientinterface; and (iii) Invasive ventilation (IV), which providesventilatory support to patients that are no longer able to effectivelybreathe themselves and may be provided using a tracheostomy tube.

1.2.3 Treatment Systems

These therapies may be provided by a treatment system or device. Suchsystems and devices may also be used to diagnose a condition withouttreating it.

A treatment system may comprise a Respiratory Pressure Therapy device(RPT device), an air circuit, a humidifier, a patient interface, anddata management.

1.2.3.1 Patient Interface

A patient interface may be used to interface respiratory equipment toits wearer, for example by providing a flow of air to an entrance to theairways. The flow of air may be provided via a mask to the nose and/ormouth, nasal pillows or cannula to the nose, a tube to the mouth or atracheostomy tube to the trachea of a patient.

1.2.3.2 Respiratory Pressure Therapy (RPT) Device

Air pressure generators are known in a range of applications, e.g.industrial-scale ventilation systems. However, air pressure generatorsfor medical applications have particular requirements not fulfilled bymore generalised air pressure generators, such as the reliability, sizeand weight requirements of medical devices. In addition, even devicesdesigned for medical treatment may suffer from shortcomings, pertainingto one or more of: comfort, noise, ease of use, efficacy, size, weight,manufacturability, cost, and reliability.

An example of the special requirements of certain RPT devices isacoustic noise.

Table of noise output levels of prior RPT devices (one specimen only,measured using test method specified in ISO 3744 in CPAP mode at 10cmH₂O).

A-weighted sound Year RPT Device name pressure level dB(A) (approx.)C-Series Tango ™ 31.9 2007 C-Series Tango ™ with Humidifier 33.1 2007 S8Escape ™ II 30.5 2005 S8 Escape ™ II with H4i ™ Humidifier 31.1 2005 S9AutoSet ™ 26.5 2010 S9 AutoSet ™ with H5i Humidifier 28.6 2010

One known RPT device used for treating sleep disordered breathing is theS9 Sleep Therapy System, manufactured by ResMed Limited. Another exampleof an RPT device is a ventilator. Ventilators such as the ResMedStellar™ Series of Adult and Paediatric Ventilators may provide supportfor invasive and non-invasive non-dependent ventilation for a range ofpatients for treating a number of conditions such as but not limited toNMD, OHS and COPD.

The ResMed Elisée™ 150 ventilator and ResMed VS III™ ventilator mayprovide support for invasive and non-invasive dependent ventilationsuitable for adult or paediatric patients for treating a number ofconditions. These ventilators provide volumetric and barometricventilation modes with a single or double limb circuit. RPT devicestypically comprise a pressure generator, such as a motor-driven bloweror a compressed gas reservoir, and are configured to supply a flow ofair to the airway of a patient. In some cases, the flow of air may besupplied to the airway of the patient at positive pressure. The outletof the RPT device is connected via an air circuit to a patient interfacesuch as those described above.

The designer of a device may be presented with an infinite number ofchoices to make. Design criteria often conflict, meaning that certaindesign choices are far from routine or inevitable. Furthermore, thecomfort and efficacy of certain aspects may be highly sensitive tosmall, subtle changes in one or more parameters.

1.2.3.3 Humidifier

Delivery of a flow of air without humidification may cause drying ofairways. The use of a humidifier with an RPT device and the patientinterface produces humidified gas that minimizes drying of the nasalmucosa and increases patient airway comfort. In addition in coolerclimates, warm air applied generally to the face area in and about thepatient interface is more comfortable than cold air. A range ofartificial humidification devices and systems are known, however theymay not fulfil the specialised requirements of a medical humidifier.

Medical humidifiers are used to increase humidity and/or temperature ofthe flow of air in relation to ambient air when required, typicallywhere the patient may be asleep or resting (e.g. at a hospital). Amedical humidifier for bedside placement may be small. A medicalhumidifier may be configured to only humidify and/or heat the flow ofair delivered to the patient without humidifying and/or heating thepatient's surroundings. Room-based systems (e.g. a sauna, an airconditioner, or an evaporative cooler), for example, may also humidifyair that is breathed in by the patient, however those systems would alsohumidify and/or heat the entire room, which may cause discomfort to theoccupants. Furthermore medical humidifiers may have more stringentsafety constraints than industrial humidifiers

While a number of medical humidifiers are known, they can suffer fromone or more shortcomings Some medical humidifiers may provide inadequatehumidification, some are difficult or inconvenient to use by patients.

Medical humidifiers typically comprise a humidifier reservoir forretaining a body of water for humidifying the flow of air, and a heatsource (e.g. a resistive heater) configured heat the body of water.Typically, heat is transferred from the heat source to the reservoir byconduction.

Construction and/or arrangement of the heat source and the humidifierreservoir to achieve appropriate thermal contact therebetween (and thusheat transfer) can be challenging. For example, air gaps formed betweenthe heat source and the heat transfer target may greatly decreasethermal contact, as air is an insulating medium (i.e. not a goodheat-conducting material).

In many prior art humidifiers, high precision, flat heater plates (heatsource) are configured to be coupled with flat conductive plates (heattarget) in a humidifier reservoir to meet thermal contact and thereforeheat transfer requirements. Typically these plates are manufactured froma conductive metal (e.g. steel or aluminium) and can be costly.

Another challenge to adequate thermal contact between the heater plateand the conductive plate is that of managing manufacturing and assemblytolerances in relation to insertion and/or retention of the reservoir inthe humidifier. In some prior art humidifiers, the heater plates and/orthe humidifier reservoir may include a spring element to bias the heaterplate and the conductive plate toward each other to improve thermalcontact therebetween.

Such prior art solutions listed above may increase material and/ormanufacturing costs of the humidifier for the manufacturer whilepotentially decreasing the manufacturing yield, which may not bedesirable. Furthermore, humidifiers reservoirs are typically disposablefor one or a plurality of reasons, such as wear, foreign matterbuild-up, regulatory and hygienic requirements, such as formulti-patient use. Thus, it is preferable for the humidifier reservoirto be a low-cost item.

1.2.3.4 Vent Technologies

Some forms of treatment systems may include a vent to allow the washoutof exhaled carbon dioxide. The vent may allow a flow of gas from aninterior space of a patient interface, e.g., the plenum chamber, to anexterior of the patient interface, e.g., to ambient. The vent maycomprise an orifice and gas may flow through the orifice in use of themask. Many such vents are noisy. Others may become blocked in use andthus provide insufficient washout. Some vents may be disruptive of thesleep of a bed partner 1100 of the patient 1000, e.g. through noise orfocussed airflow.

2 BRIEF SUMMARY OF THE TECHNOLOGY

The present technology is directed towards providing medical devicesused in the diagnosis, amelioration, treatment, or prevention ofrespiratory disorders having one or more of improved comfort, cost,efficacy, ease of use and manufacturability.

A first aspect of the present technology relates to apparatus used inthe diagnosis, amelioration, treatment or prevention of a respiratorydisorder.

Another aspect of the present technology relates to methods used in thediagnosis, amelioration, treatment or prevention of a respiratorydisorder.

One form of the present technology comprises a flexible humidifierreservoir configured to contain a body of water for humidifying a flowof pressurized breathable gas generated by a respiratory apparatus.

Another form of the present technology comprises a kit of one or morepre-filled flexible humidifier reservoirs.

Another form of the present technology comprises a flexible humidifierreservoir configured to be coupled to more than one type of humidifierAnother form of the present technology comprises a flexible humidifierreservoir that is prefilled with water for humidifying a flow ofpressurized breathable gas generated by a respiratory apparatus base.

Another form of the present technology comprises a flexible humidifierreservoir configured to be coupled to more than one type of respiratoryapparatus.

Another form of the present technology comprises a method forhumidifying a flow of pressurized breathable gas generated by arespirator apparatus.

Another aspect of the present technology comprises a method for changingthe shape of a humidifier reservoir to conform to the shape of ahumidifier base or a receiving portion of a flow generator.

Another aspect of one form of the present technology is a humidifier fora continuous positive airway pressure (CPAP) apparatus. The humidifierincludes a base unit configured to be coupled to the CPAP apparatus andcomprising a receiving space and a variable volume chamber configured tohold a body of water and receive pressurized gas from the CPAP apparatusto humidify the pressurized gas. The receiving space is configured toreceive the variable volume chamber and the variable volume chamber isconformable to a shape of the receiving space.

Another aspect of one form of the present technology is a humidifier fora continuous positive airway pressure (CPAP) apparatus. The humidifierincludes a flexible chamber configured to hold a body of water andreceive pressurized gas from the CPAP apparatus to humidify thepressurized gas and a base unit configured to support the flexiblechamber. The flexible chamber is configured to conform to a shape of areceiving space of the base unit upon being received by the base unit.

Another aspect of one form of the present technology is a humidifier fora continuous positive airway pressure (CPAP) apparatus. The humidifierincludes a conformable chamber configured to hold a body of water andreceive pressurized gas from the CPAP apparatus to humidify thepressurized gas and a retaining space configured to retain the flexiblechamber in a fixed position relative to the CPAP apparatus. The walls ofthe retaining space are configured to force the conformable chamber intoa predetermined shape upon the conformable chamber being received by theretaining space.

Another aspect of one form of the present technology is a patientinterface that is moulded or otherwise constructed with a perimetershape which is complementary to that of an intended wearer.

An aspect of one form of the present technology is a method ofmanufacturing apparatus.

An aspect of certain forms of the present technology is a medical devicethat is easy to use, e.g. by a person who does not have medicaltraining, by a person who has limited dexterity or by a person withlimited experience in using this type of medical device.

An aspect of one form of the present technology is a portable RPT devicethat may be carried by a person, e.g., around the home of the person.

An aspect of one form of the present technology is a patient interfacethat may be washed in a home of a patient, e.g., in soapy water, withoutrequiring specialised cleaning equipment. An aspect of one form of thepresent technology is a humidifier tank that may be washed in a home ofa patient, e.g., in soapy water, without requiring specialised cleaningequipment.

Of course, portions of the aspects may form sub-aspects of the presenttechnology. Also, various ones of the sub-aspects and/or aspects may becombined in various manners and also constitute additional aspects orsub-aspects of the present technology.

Other features of the technology will be apparent from consideration ofthe information contained in the following detailed description,abstract, drawings and claims.

3 BRIEF DESCRIPTION OF THE DRAWINGS

The present technology is illustrated by way of example, and not by wayof limitation, in the figures of the accompanying drawings, in whichlike reference numerals refer to similar elements including:

3.1 Treatment Systems

FIG. 1 shows a system including a patient 1000 wearing a patientinterface 3000, in the form of a nasal pillows, receiving a supply ofair at positive pressure from an RPT device 4000. Air from the RPTdevice is humidified in a humidifier 5000, and passes along an aircircuit 4170 to the patient 1000. A bed partner 1100 is also shown.

3.2 Respiratory System and Facial Anatomy

FIG. 2 shows an overview of a human respiratory system including thenasal and oral cavities, the larynx, vocal folds, oesophagus, trachea,bronchus, lung, alveolar sacs, heart and diaphragm.

3.3 Patient Interface

FIG. 3 shows a patient interface in the form of a nasal mask inaccordance with one form of the present technology.

3.4 RPT Device

FIG. 4A shows an RPT device in accordance with one form of the presenttechnology.

FIG. 4B is a schematic diagram of the pneumatic path of an RPT device inaccordance with one form of the present technology. The directions ofupstream and downstream are indicated.

FIG. 4C is a schematic diagram of the electrical components of an RPTdevice in accordance with one form of the present technology.

3.5 Humidifier

FIG. 5A shows an isometric view of a humidifier in accordance with oneform of the present technology.

FIG. 5B shows an isometric view of a humidifier in accordance with oneform of the present technology.

FIG. 5C shows a humidifier in accordance with one form of the presenttechnology.

FIG. 5D shows a flexible reservoir according to one form of the presenttechnology.

FIG. 5E shows a flexible reservoir according to one form of the presenttechnology.

FIG. 5F shows a flexible reservoir according to one form of the presenttechnology.

FIG. 5G shows a flexible reservoir according to one form of the presenttechnology.

FIG. 5H shows a flexible reservoir according to one form of the presenttechnology.

FIG. 5I shows a flexible reservoir according to one form of the presenttechnology.

FIG. 5J shows a flexible reservoir according to one form of the presenttechnology.

FIG. 5K shows a flexible reservoir according to one form of the presenttechnology.

FIG. 5L shows a flexible reservoir according to one form of the presenttechnology.

FIG. 5M shows an air inlet of a flexible reservoir according to one formof the present technology.

FIG. 5N shows an air inlet of a flexible reservoir according to one formof the present technology.

FIG. 5O shows a flexible reservoir according to one form of the presenttechnology.

FIG. 5P shows a flexible reservoir according to one form of the presenttechnology.

FIG. 5Q shows a travel kit according to one form of the presenttechnology.

FIG. 5R shows a flexible reservoir according to one form of the presenttechnology.

FIG. 5S shows a flexible reservoir according to one form of the presenttechnology.

FIG. 5T shows a flexible reservoir according to one form of the presenttechnology.

FIG. 5U shows a flexible reservoir according to one form of the presenttechnology.

4 DETAILED DESCRIPTION OF EXAMPLES OF THE TECHNOLOGY

Before the present technology is described in further detail, it is tobe understood that the technology is not limited to the particularexamples described herein, which may vary. It is also to be understoodthat the terminology used in this disclosure is for the purpose ofdescribing only the particular examples discussed herein, and is notintended to be limiting.

The following description is provided in relation to various exampleswhich may share one or more common characteristics and/or features. Itis to be understood that one or more features of any one example may becombinable with one or more features of another example or otherexamples. In addition, any single feature or combination of features inany of the examples may constitute a further example.

4.1 THERAPY

In one form, the present technology comprises a method for treating arespiratory disorder comprising the step of applying positive pressureto the entrance of the airways of a patient 1000.

In certain examples of the present technology, a supply of air atpositive pressure is provided to the nasal passages of the patient viaone or both nares.

In certain examples of the present technology, mouth breathing islimited, restricted or prevented.

4.2 TREATMENT SYSTEMS

In one form, the present technology comprises an apparatus or device fortreating a respiratory disorder. The apparatus or device may comprise anRPT device 4000 for supplying pressurised air to the patient 1000 via anair circuit 4170 to a patient interface 3000.

4.3 PATIENT INTERFACE

A non-invasive patient interface 3000 in accordance with one aspect ofthe present technology comprises the following functional aspects: aseal-forming structure 3100, a plenum chamber 3200, a positioning andstabilising structure 3300, a vent 3400, one form of connection port3600 for connection to air circuit 4170, and a forehead support 3700. Insome forms a functional aspect may be provided by one or more physicalcomponents. In some forms, one physical component may provide one ormore functional aspects. In use the seal-forming structure 3100 isarranged to surround an entrance to the airways of the patient so as tofacilitate the supply of air at positive pressure to the airways.

Examples of non-invasive patient interfaces according to one aspect ofthe present technology include a nasal mask, a nose and mouth mask and anasal cannula. An example of an invasive patient interface according toone aspect of the present technology includes a tracheostomy tube.

4.4 RPT DEVICE

An RPT device 4000 in accordance with one aspect of the presenttechnology comprises mechanical and pneumatic components 4100,electrical components 4200 and is configured to execute one or morealgorithms. The RPT device may have an external housing 4010, formed intwo parts, an upper portion 4012 and a lower portion 4014. Furthermore,the external housing 4010 may include one or more panel(s) 4015. The RPTdevice 4000 comprises a chassis 4016 that supports one or more internalcomponents of the RPT device 4000. The RPT device 4000 may include ahandle 4018.

The pneumatic path of the RPT device 4000 may comprise one or more airpath items, e.g., an inlet air filter 4112, an inlet muffler 4122, apressure generator 4140 capable of supplying air at positive pressure(e.g., a blower 4142), an outlet muffler 4124 and one or moretransducers 4270, such as pressure sensors 4272 and flow rate sensors4274.

One or more of the air path items may be located within a removableunitary structure which will be referred to as a pneumatic block 4020.The pneumatic block 4020 may be located within the external housing4010. In one form the pneumatic block 4020 is supported by, or formed aspart of the chassis 4016.

The RPT device 4000 may have an electrical power supply 4210, one ormore input devices 4220, a central controller 4230, a therapy devicecontroller 4240, a pressure generator 4140, one or more protectioncircuits 4250, memory 4260, transducers 4270, data communicationinterface 4280 and one or more output devices 4290. Electricalcomponents 4200 may be mounted on a single Printed Circuit BoardAssembly (PCBA) 4202. In an alternative form, the RPT device 4000 mayinclude more than one PCBA 4202.

4.4.1 RPT Device Mechanical & Pneumatic Components

An RPT device may comprise one or more of the following components in anintegral unit. In an alternative form, one or more of the followingcomponents may be located as respective separate units.

4.4.1.1 Air Filter(s)

An RPT device in accordance with one form of the present technology mayinclude an air filter 4110, or a plurality of air filters 4110.

In one form, an inlet air filter 4112 is located at the beginning of thepneumatic path upstream of a pressure generator 4140. See FIG. 4B.

In one form, an outlet air filter 4114, for example an antibacterialfilter, is located between an outlet of the pneumatic block 4020 and apatient interface 3000. See FIG. 4B.

4.4.1.2 Muffler(s)

In one form of the present technology, an inlet muffler 4122 is locatedin the pneumatic path upstream of a pressure generator 4140. See FIG.4B.

In one form of the present technology, an outlet muffler 4124 is locatedin the pneumatic path between the pressure generator 4140 and a patientinterface 3000. See FIG. 4B.

4.4.1.3 Pressure Generator

In one form of the present technology, a pressure generator 4140 forproducing a flow, or a supply, of air at positive pressure is acontrollable blower 4142. For example the blower 4142 may include abrushless DC motor 4144 with one or more impellers housed in a volute.The blower may be capable of delivering a supply of air, for example ata rate of up to about 120 liters/minute, at a positive pressure in arange from about 4 cmH₂O to about 20 cmH₂O, or in other forms up toabout 30 cmH₂O. The blower may be as described in any one of thefollowing patents or patent applications the contents of which areincorporated herein by reference in their entirety: U.S. Pat. No.7,866,944; U.S. Pat. No. 8,638,014; U.S. Pat. No. 8,636,479; and PCTPatent Application Publication No. WO 2013/020167.

The pressure generator 4140 is under the control of the therapy devicecontroller 4240.

In other forms, a pressure generator 4140 may be a piston-driven pump, apressure regulator connected to a high pressure source (e.g. compressedair reservoir), or a bellows.

4.4.1.4 Transducer(s)

Transducers may be internal of the RPT device, or external of the RPTdevice. External transducers may be located for example on or form partof the air circuit, e.g., the patient interface. External transducersmay be in the form of non-contact sensors such as a Doppler radarmovement sensor that transmit or transfer data to the RPT device.

In one form of the present technology, one or more transducers 4270 arelocated upstream and/or downstream of the pressure generator 4140. Theone or more transducers 4270 may be constructed and arranged to measureproperties such as a flow rate, a pressure or a temperature at thatpoint in the pneumatic path.

In one form of the present technology, one or more transducers 4270 maybe located proximate to the patient interface 3000.

In one form, a signal from a transducer 4270 may be filtered, such as bylow-pass, high-pass or band-pass filtering.

4.4.1.4.1 Flow Rate Sensor

A flow rate sensor 4274 in accordance with the present technology may bebased on a differential pressure transducer, for example, an SDP600Series differential pressure transducer from SENSIRION.

In one form, a signal representing a flow rate such as a total flow rateQt from the flow rate sensor 4274 is received by the central controller4230.

4.4.1.4.2 Pressure Sensor

A pressure sensor 4272 in accordance with the present technology islocated in fluid communication with the pneumatic path. An example of asuitable pressure transducer is a sensor from the HONEYWELL ASDX series.An alternative suitable pressure transducer is a sensor from the NPASeries from GENERAL ELECTRIC.

In one form, a signal from the pressure sensor 4272 is received by thecentral controller 4230.

4.4.1.4.3 Motor Speed Transducer

In one form of the present technology a motor speed transducer 4276 isused to determine a rotational velocity of the motor 4144 and/or theblower 4142. A motor speed signal from the motor speed transducer 4276may be provided to the therapy device controller 4240. The motor speedtransducer 4276 may, for example, be a speed sensor, such as a Halleffect sensor.

4.4.1.5 Anti-Spill Back Valve

In one form of the present technology, an anti-spill back valve 4160 islocated between the humidifier 5000 and the pneumatic block 4020. Theanti-spill back valve 4160 is constructed and arranged to reduce therisk that water will flow upstream from the humidifier 5000, for exampleto the motor 4144.

4.4.1.6 Oxygen Delivery

In one form of the present technology, supplemental oxygen 4180 isdelivered to one or more points in the pneumatic path, such as upstreamof the pneumatic block 4020, to the air circuit 4170 and/or to thepatient interface 3000.

4.4.2 RPT Device Electrical Components

4.4.2.1 Power Supply

A power supply 4210 may be located internal or external of the externalhousing 4010 of the RPT device 4000.

In one form of the present technology, power supply 4210 provideselectrical power to the RPT device 4000 only. In another form of thepresent technology, power supply 4210 provides electrical power to bothRPT device 4000 and humidifier 5000.

4.4.2.2 Input Devices

In one form of the present technology, an RPT device 4000 includes oneor more input devices 4220 in the form of buttons, switches or dials toallow a person to interact with the device. The buttons, switches ordials may be physical devices, or software devices accessible via atouch screen. The buttons, switches or dials may, in one form, bephysically connected to the external housing 4010, or may, in anotherform, be in wireless communication with a receiver that is in electricalconnection to the central controller 4230.

In one form, the input device 4220 may be constructed and arranged toallow a person to select a value and/or a menu option.

4.4.2.3 Central Controller

In one form of the present technology, the central controller 4230 isone or a plurality of processors suitable to control an RPT device 4000.

4.4.2.4 Clock

The RPT device 4000 may include a clock 4232 that is connected to thecentral controller 4230.

4.4.2.5 Therapy Device Controller

In one form of the present technology, therapy device controller 4240 isa therapy control module that forms part of the algorithms executed bythe central controller 4230.

4.4.2.6 Data Communication Systems

In one form of the present technology, a data communication interface4280 is provided, and is connected to the central controller 4230. Datacommunication interface 4280 may be connectable to a remote externalcommunication network 4282 and/or a local external communication network4284. The remote external communication network 4282 may be connectableto a remote external device 4286. The local external communicationnetwork 4284 may be connectable to a local external device 4288.

4.4.2.7 Output Devices Including Optional Display, Alarms

An output device 4290 in accordance with the present technology may takethe form of one or more of a visual, audio and haptic unit. A visualdisplay may be a Liquid Crystal Display (LCD) or Light Emitting Diode(LED) display.

4.4.2.7.1 Display Driver

A display driver 4292 receives as an input the characters, symbols, orimages intended for display on the display 4294, and converts them tocommands that cause the display 4294 to display those characters,symbols, or images.

4.4.2.7.2 Display

A display 4294 is configured to visually display characters, symbols, orimages in response to commands received from the display driver 4292.For example, the display 4294 may be an eight-segment display, in whichcase the display driver 4292 converts each character or symbol, such asthe figure “0”, to eight logical signals indicating whether the eightrespective segments are to be activated to display a particularcharacter or symbol.

4.5 AIR CIRCUIT

An air circuit 4170 in accordance with an aspect of the presenttechnology is a conduit or a tube constructed and arranged in use toallow a flow of air to travel between two components such as between thepneumatic block 4020 and the patient interface 3000, between the RPTdevice 4000 and the humidifier 5000, or between the humidifier 5000 andthe patient interface 3000.

In particular, the air circuit 4170 may be in fluid connection with theoutlet of the pneumatic block and the patient interface. The air circuitmay be referred to as an air delivery tube. In some cases there may beseparate limbs of the circuit for inhalation and exhalation. In othercases a single limb is used. An air circuit may be a part of an RPTdevice 4000 in some forms, although it may be a separate component inother forms.

In some forms, the air circuit 4170 may comprise one or more heatingelements configured to heat air in the air circuit, for example tomaintain or raise the temperature of the air. The heating element may bein a form of a heated wire circuit, and may comprise one or moretransducers, such as temperature sensors. In one form, the heated wirecircuit may be helically wound around the axis of the air circuit 4170.The heating element may be in communication with a controller such as acentral controller 4230. One example of an air circuit 4170 comprising aheated wire circuit is described in United States Patent Application No.US/2011/0023874, which is incorporated herewithin in its entirety byreference.

4.6 HUMIDIFIER

4.6.1 Humidifier Overview

In one form of the present technology there is provided a humidifier5000 (e.g. as shown in FIGS. 5A-|5C|_([JPH1])) to change the temperatureand/or the absolute humidity of air or gas for delivery to a patientrelative to ambient air. Typically, the humidifier 5000 is used toincrease the absolute humidity and increase the temperature of the flowof air (e.g. relative to ambient air) before delivery to the patient'sairways.

The humidifier 5000 may comprise a humidifier reservoir 5110, ahumidifier inlet 5002 to receive a flow of air, and a humidifier outlet5004 to deliver a humidified flow of air. In some forms, as shown inFIG. 5C, an inlet and an outlet of the humidifier reservoir 5110 may bethe humidifier inlet 5002 and the humidifier outlet 5004 respectively.The humidifier 5000 may further comprise a humidifier base 5006, whichmay be adapted to receive the humidifier reservoir 5110 and comprise aheating element (also referred to as a heater)(not shown).

In some forms, a humidifier 5000 may be separably configured withrespect to the RPT device 4000. For example, the humidifier may bedetachably connected to a housing of the RPT device 4000, or detachablyconnected via an air circuit. In other forms, a humidifier 5000 and anRPT device 4000 may be integrally constructed as a single apparatus orassembly.

4.6.2 Humidifier Mechanical Components

4.6.2.1 Humidifier Base_([JPH2])

The humidifier 5000 may comprise a humidifier base 5006 in some forms ofthe present technology. The humidifier base 5006 may comprise one ormore components, such as: a receiving space 5112, a heating element (notshown), a flow sensor, a temperature sensor, a humidity sensor, apressure sensor and/or a humidifier controller 5176. The humidifier base5006 may comprise a housing enclosing one or more components. Thehumidifier base 5006 may be configured for example to provide a rigidstructure for the humidifier 5000.

In some forms, the humidifier base 5006 may be configured to couple to,or receive, the humidifier reservoir 5110 to locate and/or secure thehumidifier reservoir 5110.

The humidifier base 5006 may be located at or near a lower portion ofthe humidifier 5000 as shown in FIG. 5A or FIG. 5B. However, the term‘humidifier base’, as used in the present document will be understood tobe not limiting in terms of location with respect to the rest of thehumidifier 5000. For example, the humidifier base may be locatedprimarily on a side, top, or a bottom of the humidifier 5000 whenoriented in a normal working, upright, orientation.

4.6.2.2 Humidifier Reservoir

According to one arrangement, the humidifier 5000 may comprise areservoir 5110 configured to hold, or retain, a volume of liquid (e.g.water) to be evaporated for humidification of the flow of air. Thereservoir 5110 may be configured to hold a predetermined maximum volumeof water (or any other suitable liquid) in order to provide adequatehumidification for at least the duration of a respiratory therapysession, such as one evening of sleep. Typically, the reservoir 5110 isconfigured to hold several hundred milliliters of water, e.g. 300milliliters (ml), 325 ml, 350 ml or 400 ml. It is contemplated that insome forms, a humidifier reservoir 5110 may be larger or smaller.

According to one aspect, the reservoir 5110 is configured to addhumidity to a flow of air from the RPT device 4000 as the flow of airtravels therethrough. In one form, the reservoir 5110 may be configuredto encourage the flow of air to travel in a tortuous path through thereservoir 5110 while in contact with the volume of water therein.

The reservoir 5110 may be constructed from a pliant, flexible materialsuch as, for example, polyethylene, polyamide or a combination thereof.It is contemplated that the reservoir 5110 may be made of other plasticsor other flexible and bio-compatible materials in combination with or insubstitution of the polyethylene and polyamide. As such, the reservoir5110 may conform to the shape of the receiving space 5112 of thehumidifier 5000 for example in use.

It will be understood that the walls of the reservoir 5110 may be sizedto achieve sufficiently pliant and conformal behaviour and other designrequirements such as resistance to breakage and/or deformation. Forexample, for a first material comprising a higher elastic modulus and ahigher yield strength than a second material, a smaller wall thicknessmay be suitable while achieving similar mechanical properties.

The humidifier 5000 may comprise one or more walls defining thereceiving space 5112. The receiving space 5112 may be configured toreceive the reservoir 5110, and for example may be located in thehumidifier base 5006. It will be understood that a variety of shapes maybe suitable for the receiving space 5112. For example, the set of wallsmay be orthogonally arranged as to define a prism shaped receiving space5112 as shown in FIG. 5A, or define a non-prism shaped receiving space5112 as shown in FIG. 5B. It is further contemplated that the set ofwalls may be curved to define a hemispherical receiving space 5112 (notshown). In addition, the pliant nature of the reservoir 5110 may allowfor the reservoir 5110 be used with more than one type of humidifier5000 or RPT device 4000, such as to suit a plurality of shapes of thereceiving space 5112. Such a design may be beneficial for amanufacturer, distributor and consumer alike for example, as it mayreduce manufacturing burden, inventory, costs and likelihood of wastage.

It should be understood that in configurations where the reservoir 5110is received directly by the RPT device 4000, the receiving space 5112may be defined by one or more walls of the RPT device 4000.

The reservoir 5110 may also be structured to exist in a plurality ofconfigurations. For example, the reservoir 5110 may be convertiblebetween a storage (or transport) configuration and a workingconfiguration. The reservoir 5110 in the storage configuration may becollapsed, folded and/or rolled for example to reduce its volume. Insome forms, the reservoir 5110 may be collapsible to a flat plate forimproved stacking with other collapsed reservoirs.

In some forms, a plurality of reservoirs 5110 may be stored togetherwith (for example inside) the humidifier 5000, such that a kit may beprovided for convenient storage, sale and transport. For example, aplurality of reservoirs 5110 in their storage configurations may bestored in the humidifier 5000, such as in the receiving space 5112 toreduce the volume for transport or another storage compartment for eachaccess by the patient.

In the working configuration, the reservoir 5110 may comprise anincreased volume, such as expanded by the patient, receipt of a volumeof water and/or a flow of air. Thus, the reservoir 5110 may expand toconform to a shape of the receiving space 5112, such as during use orwhen filled with water.

In addition, as shown in FIG. 5C, a humidifier 5000 may not comprise ahumidifier base. In some forms of the present technology, the reservoir5110 may be directly coupled to the RPT device 4000 by way of aconnector (e.g. an ISO connector) connecting the outlet of the RPTdevice 4000 to the inlet of the reservoir 5110. It is also contemplatedthat additional coupling mechanisms such as adhesive, tabs, grooves,clips, notches, frames, etc., may be used to couple the reservoir 5110directly to the RPT device 4000. Of course, the reservoir 5110 may befluidly connected to the RPT device via an air circuit 4170.

4.6.2.2.1 Humidifier Reservoir Shape

FIGS. 5A-5U illustrate reservoirs 5110 having rectangular and circularshapes in one or more cross-sections. However, the shape of thereservoir 5110 need not be limited to those illustrated in FIGS. 5A-5Tor those explicitly described herewithin. For example, the reservoir5110 may comprise one or more of triangular, cylindrical, pyramidal,prismatic or any polygonal shapes, in cross-section, elevation and/orplan views for example. It should be noted that the shape of thereservoir 5110 may be dictated by the shape of the receiving space 5112.In particular, the shape of the reservoir 5110 may be chosen to maximizethe surface area of the reservoir 5110 in direct contact with the wallsof the receiving space 5112 when the reservoir 5110 is received by thereceiving space 5112 and in use.

4.6.2.2.2 Humidifier Reservoir Engaging Portion

As shown in FIGS. 5D and 5E, the reservoir 5110 may include an engagingportion 5114. The engaging portion 5114 can facilitate positioningand/or fastening of the reservoir 5110 with respect to the humidifier5000. For example, engaging portion 5114 may position the reservoir 5110within the receiving space 5112 and/or fasten the reservoir 5110 to acomplementarily shaped portion of the receiving space 5112. The engagingportion 5114 may be, for example, one or more tabs, grooves, clips,notches, frames or any other mechanism capable of removably positioningand/or securing the reservoir 5110 to the humidifier base 5006. Thefastening (or securing) may be releasable in some forms of the presenttechnology such that the water reservoir 5110 may be replaced.

In one example, the engaging portion 5114 may be a tab configured to beinserted (e.g. by sliding) into a complementary slot in the humidifierbase 5006 (not shown). The tab may be then releasably clamped in theslot to locate and secure the reservoir 5110 with respect to thehumidifier 5000.

It is contemplated that adhesive may be provided on one or more surfacesof the reservoir 5110 (in addition to or instead of the engaging portion5114) to secure the reservoir 5110 to the humidifier base 5006. Inaddition, the reservoir 5110 may include sensors (or transducers) 5116to interact with sensors on the humidifier base 5006 for determining thepresence of the reservoir 5110. It should be understood that theengaging portion 5114 may be configured to directly couple with the RPTdevice 4000 in accordance with the configuration shown in FIG. 5C.

4.6.2.2.3 Humidifier Reservoir Inlet and Outlet

As illustrated in FIGS. 5D and 5E, the reservoir 5110 may have an airinlet 5118 and an air outlet 5120. The air inlet 5118 and the air outlet5120 may be oriented in the same direction as illustrated in FIG. 5D.Alternatively, the air inlet 5118 and the air outlet 5120 may beoriented in different directions as illustrated in FIG. 5E. In addition,the air inlet 5118 and air outlet 5120 may be projections from a mainbody 5122 (e.g. as shown in FIG. 5E). Alternatively, one or both of theair inlet 5118 and the air outlet 5120 may simply be apertures in themain body 5122.

One or both of the air inlet 5118 and the air outlet 5120 may becollapsible. For example, both of the air inlet 5118 and the air outlet5120 may be collapsible such that the entire reservoir 5110 may becollapsed into the storage configuration. In some forms, the reservoir5110 may be partly collapsible such that one or both of the air inlet5118 and the air outlet 5120 may not be collapsed in the storageconfiguration. For example, the air inlet 5118 and the air outlet 5120may be configured as rigid tubular structures.

The air inlet 5118 illustrated in FIGS. 5D and 5E may be configured tobe inserted into a connector 5124 of the humidifier base 5006 (as shownin FIG. 5B) or an outlet of the RPT device 4000. Alternatively, the airinlet 5118 may be configured to receive the connector 5124 of thehumidifier base 5006 or the outlet of the RPT device 4000. It is alsocontemplated that the air inlet 5118 may not be inserted into or receivethe connector 5124 of the humidifier base 5006 or the outlet of the RPTdevice 4000. Instead, the air inlet 5118 may be configured to engage thehumidifier base 5006 or the RPT device 4000 as a face seal. The faceseal may be pressure activated, for example be configured to establish aseal, or to increase a sealing force upon an increase in interiorpressure, such as when therapy is initiated. The face seal may comprisea bellows portion, for example any one of those described in U.S. Pat.No. 8,544,465, the contents of which are incorporated herewithin byreference.

In one form, the air inlet 5118 may comprise a face configured to engagea compliant portion (e.g. a bellows portion) located on humidifier base5006 or the RPT device 4000. In this configuration, the compliantportion would abut the face on the reservoir 5110 surrounding the airinlet 5118 to form a face seal, thereby sealing the air path. It isfurther contemplated that the air inlet 5118 may comprise a compliantportion (e.g. a bellows portion) configured to abut against acomplementary face located on the humidifier base 5006 and/or the RPTdevice 4000 to form a face seal.

Similar to the air inlet 5118, the air outlet 5120 illustrated in FIGS.5D and 5E may be configured to be inserted into a connector 5126 of thehumidifier base 5006 (as shown in FIG. 5A) or an air delivery tube (notshown). Alternatively, the air outlet 5120 may be configured to receivethe connector 5126 of the humidifier base 5006 or the air delivery tube.

In some forms, the air inlet 5118 and/or the air outlet 5120 maycomprise an ISO standard connector, such as for connecting to ahumidifier base 5006, the RPT device 4000 or an air circuit 4170. TheISO standard connector may be as specified in ISO 5356-1:2015Anaesthetic and respiratory equipment—Conical connectors—Part 1—Conesand sockets, for example comprising a 15 mm diameter or a 22 mmdiameter.

It is also contemplated that the air outlet 5120 may not be insertedinto or receive the connector 5126 of the humidifier base 5006. Instead,the air outlet 5120 may comprise a compliant portion (e.g. a bellowsportion) configured to engage the humidifier base 5006 to form a faceseal. In this configuration, the compliant portion (e.g. a bellowsportion) would abut a portion of the reservoir 5110 surrounding the airoutlet 5120 to form a sealed air path. It is further contemplated thatthe air outlet 5120 may comprise a compliant portion (e.g. a bellowsportion) configured to abut against a face of the humidifier base 5006to form a face seal.

FIGS. 5A-5F show the reservoir 5110 with one air inlet 5118 and one airoutlet 5120. In those configurations, liquid may be poured into thereservoir 5110 through either of the air inlet 5118 and the air outlet5120. However, as shown in FIG. 5G, the reservoir 5110 may include aport 5136 in addition to the air inlet 5118 and the air outlet 5120. Theport 5136 may function as an inlet/outlet for liquid. In anotherconfiguration (shown in FIG. 5H), the reservoir 5110 may include onlyone opening 5138 to act as the air inlet, the air outlet and forsupplying the reservoir 5110 with water.

4.6.2.2.4 Humidifier Reservoir Assembly

As illustrated in FIGS. 5D and 5E, the reservoir 5110 may comprise asingle unitary main body 5122 configured to substantially enclose theinterior volume of the reservoir 5110. Alternatively, as shown in FIG.5F, the main body 5122 of the reservoir 5110 may be disassembled to aplurality of components.

In one form, the main body 5122 may comprise a top portion 5128 and abottom portion 5130 removably secured to each other by way of any numberof securing mechanisms 5132 including but not limited to snap fitconnections, zip-lock sealing zipper, etc. The main body 5122 mayfurther comprise a seal 5134 sandwiched between the top portion 5128 andthe bottom portion 5130. Of course, it will be understood that the mainbody 5122 may be configured in any number of ways that allowsdisassembly into a plurality of components.

The reservoir 5110 may be disassembled, for example, into rigidcomponents and flexible components. Additionally, or alternatively, thereservoir 5110 may be disassembled into reusable and disposablecomponents. In some forms the reservoir 5110 may be disassembled suchthe plurality of disassembled components may be more readily packaged,such as for storage (or transport). In one form, the reservoir 5110 maydisassemble into a plurality of components, wherein a first componentmay be complementary to, nested in, or engage with, a second component,to a storage configuration (e.g. collapsed, flattened, rolled or folded)different to the in-use configuration of the reservoir 5110.

4.6.2.2.5 Humidifier Reservoir Inflation and Deflation

As shown in FIGS. 5I and 5K, the reservoir 5110 may initially be in adeflated condition, such as during storage and/or transport. Thereservoir 5110 may inflate or expand (FIGS. 5J and 5L) upon supplyingthe reservoir 5110 with water and/or pressurized gas. The pressurizedgas may be supplied during a therapy session.

In addition, the expansion of the reservoir 5110 (due to the addition ofliquid and/or the addition of pressurized gas) may form and/or reinforcethe seal between the air inlet 5118 and the connector 5124 of thehumidifier base 5006 as well as the seal between the air outlet 5120 andthe connector 5126 of the humidifier base 5006. For example, theexpansion of the reservoir 5110 may bias the air inlet 5118 against theconnector 5124 of the humidifier base 5006 and may bias the air outlet5120 against the connector 5126 of the humidifier base 5006. It iscontemplated that the force exerted by the expansion of the reservoir5110 may also prevent the connection between the air inlet 5118 and theconnector 5124 of the humidifier base 5006 from being broken and mayprevent the connection between the air outlet 5120 and the connector5126 of the humidifier base 5006 from being broken.

The expansion of the reservoir 5110 may also bias the main body 5122against an interior surface of the receiving space 5112. The expansionof the reservoir 5110 may locate the main body 5122 in a workingposition within the receiving space 5112, and/or engage the main body5122 with respect to the receiving space 5112 such that the reservoir5110 may be frictionally secured to the humidifier base 5006 due to theforce exerted by the expansion of the reservoir 5110.

4.6.2.2.6 Humidifier Reservoir Backflow Prevention

It is contemplated that the reservoir 5110 may also include a backflow(spillback) prevention system for preventing the flow of liquid throughthe air inlet 5118. For example, as illustrated in FIGS. 5J and 5K, thereservoir 5110 may include a divider 5140 to prevent liquid flowingthrough the air inlet 5118. The divider 5140 may divide the reservoir5110 into two chambers (i.e., a first chamber 5142 and a second chamber5144). In addition, as shown in FIG. 5L, an opening 5146 in the divider5140 may allow pressurized gas to communicate with both the first andsecond chambers 5142, 5144. The opening 5146 may be located as far awayfrom the air inlet 5118 as possible, such as at or near a geometriccentre of the main body 5122. Such a configuration may have the effectof allowing the reservoir to rotate from an “in use” position and stillprevent liquid from flowing through the air inlet 5118. It should benoted that in this configuration, the air outlet 5120 may be the outletof the second chamber 5144.

As shown in FIG. 5K, the divider 5140 may not have an opening. Instead,the divider 5140 may be comprised of a gas permeable membrane thatallows pressurized gas and water vapor to flow through the divider 5140but prevents liquid from flowing through the divider 5140. In thisconfiguration, the reservoir 5110 may be prefilled with liquid or liquidmay be supplied and drained by way of the port 5136 formed adjacent thesecond chamber 5144.

In addition, the divider 5140 may have the same flexibility as the restof the reservoir 5110. For example, the divider 5140 may be formed fromthe same material as the exterior walls of the reservoir 5110.Alternatively, the divider 5140 may be more rigid than the rest of thereservoir 5110. In the “more rigid” configuration, the divider 5140 mayprovide structural support to the reservoir 5110 so that the reservoir5110 may be both conformable to the humidifier base 5006 and be able tomaintain some basic shape when removed from the humidifier base 5006.

As illustrated in FIGS. 5M and 5N, the air inlet 5118 may include acheck valve 5148 biased in the closed position. The check valve 5148 maybe configured so that a predetermined pressure overcomes the biasingforce maintaining the check valve 5148 in the closed position. Thepredetermined pressure may have the effect of opening the check valve5148 and preventing the liquid in the reservoir 5110 from flowingthrough the air inlet 5118.

It is contemplated that the check valve 5148 may also be configured toseal the air inlet 5118 when the reservoir 5110 is separated from thehumidifier base 5006. In this configuration, insertion of the connector5124 of the humidifier base 5006 may push the check valve 5148 open whenthe connector 5124 of the humidifier base 5006 is inserted into the airinlet 5118.

It is further contemplated that the air inlet 5118 may have multiplecheck valves 5148 and that the multiple check valves 5148 may bepositioned in series with each other. The outermost check valve 5148 maybe configured to open when the connector 5124 of the humidifier base5006 is inserted into the air inlet 5118 and the additional one or morecheck valves 5148 in the air inlet 5118 may be configured to open whenthe predetermined air pressure is provided to the air inlet 5118.

It should be noted that although only the check valve and dividerconfigurations have been disclosed above with respect to backflowprevention, the backflow prevention system is not limited to theconfigurations discussed above.

4.6.2.2.7 Humidifier Reservoir Rigidizing Structures

As can be seen in FIGS. 5O and 5P, the reservoir 5110 may includeinternal and/or external rigidizing structures to provide additional ofrigidity to the reservoir 5110, for example to the main body 5122. Therigidizing structure may be in the form of one or more ribs 5150extending across an internal surface of the reservoir 5110. The one ormore ribs 5150 may extend completely across the reservoir 5110 or mayonly extend across a portion of the reservoir 5110. In addition, theribs 5150 may form any type of pattern that would result in a particularcharacteristic of rigidity. For example, the ribs 5150 may be positionedto provide rigidity one direction while allowing for completeconformability in a second direction.

As discussed above, the reservoir 5110 may include an external structureto provide some level of rigidity to the reservoir 5110. For example,the external structure may be an exoskeleton 5152. Similar to the one ormore ribs 5150, the exoskeleton 5152 may be provided in any number ofpatterns designed to provide a particular characteristic of rigidity.For example, the exoskeleton 5152 may be configured to provide asignificantly higher rigidity in one direction than in a second,orthogonal, direction, thus allowing conformability in the seconddirection.

4.6.2.2.8 Humidifier Reservoir Kit

It is contemplated that the reservoir 5110 may be packaged as a kit tobe used with one or more types of humidifier base 5006. The packagedreservoir 5110 may be provided with or without water. In addition, eachpackaged kit may include one or more prefilled or non-prefilledreservoirs 5110. The kits could be provided in their collapsed form inorder to be stackable and allow for bulk transport.

For example, the reservoir 5110 may be configured to be folded orotherwise manipulated to a travel configuration. The reservoir 5110 maybe folded, rolled, wrapped, flattened or otherwise reduced in size(e.g., in volume and/or cross-section areas), for example to be fittedinto the RPT device 4000, or a travel bag.

An exemplary travel kit is illustrated in FIG. 5Q and may comprise atravel bag 5167 including a first receptacle 5168 configured to receivethe RPT device 4000, and a second receptacle 5170 configured to receivethe reservoir 5110 in its travel configuration, wherein a volume of thereservoir 5110 (and the volume of the second receptacle 5170) may besmaller than the volume of the reservoir 5110 in its working, expandedconfiguration. A securement strap 5172 may retain the RPT device 4000 inthe first receptacle 5168.

In one example, the first receptacle 5168 may comprise a cavity shapedas a prism to receive an RPT device 4000 and the second receptacle 5170may comprise a slot-shaped cavity configured to receive the reservoir5110 in its travel configuration.

In some forms, the travel bag 5167 may be additionally configured toreceive the humidifier base 5006 in a third receptacle 5174. Asecurement strap 5175 may retain the humidifier base 5006 in the thirdreceptacle 5174. In either configuration, the humidifier base 5006and/or the RPT device 4000 may be configured to store the reservoir 5110in its travel configuration in lieu of the second receptacle 5170described above.

In addition, reservoirs 5110 provided in kits may include frames 5154(as illustrated in FIG. 5R) with engagable portions configured to securethe reservoir 5110 to the humidifier base 5006 prior to expansion of thereservoir 5110. In addition, kits may be matched with particular CPAPunits or be configured to be used with multiple types of CPAP units.Also, the kits may include different versions of the reservoir 5110 withdifferent levels of durability. More durable reservoirs 5110 would besuitable for travel.

In addition, or as an alternative, prior to first use, the air inlet5118 and/or the air outlet 5120 may be sealed by, for example, frangibleseals and/or perforations that could be opened for use. It iscontemplated that the seal could be punctured by the insertion of theconnector 5124 of the humidifier base 5006 into the air inlet 5118. Inaddition, the air outlet seal could be punctured by inserting theconnector 5126 of the humidifier base 5006 into the air outlet 5120 orsecuring an air delivery tube to the air outlet 5120.

It is contemplated that the reservoir 5110 may be a single-use reservoiror a multi-use reservoir.

According to one form, the reservoir 5110 may be removable from thehumidifier 5000, for example in a lateral direction as shown in FIG. 5Aand FIG. 5B.

The reservoir 5110 may also be configured to discourage egress of liquidtherefrom, such as when the reservoir 5110 is displaced and/or rotatedfrom its normal, working orientation, such as through any aperturesand/or in between its sub-components. As the flow of air to behumidified by the humidifier 5000 is typically pressurised, thereservoir 5110 may also be configured to prevent losses in pneumaticpressure through leak and/or flow impedance.

4.6.2.3 Conductive Portion

According to one arrangement as illustrated in FIG. 5S, the reservoir5110 may comprise a conductive portion 5156 configured to allowefficient transfer of heat from a heating element (not shown) of thehumidifier base 5006 to the volume of liquid in the reservoir 5110. Inone form, the conductive portion 5156 may be arranged as a plate,although other shapes may also be suitable. In addition, the conductiveportion 5156 may be located on a bottom surface of the main body 5122 ofthe reservoir 5110. All or a part of the conductive portion 5156 may bemade of a thermally conductive material such as aluminium (e.g.approximately 2 mm thick, such as 1 mm, 1.5 mm, 2.5 mm or 3 mm), anotherheat conducting metal or some plastics. In some cases, suitable heatconductivity may be achieved with less conductive materials of suitablegeometry.

In addition, the conductive portion 5156 may be more rigid than the restof the reservoir 5110. As such, the conductive portion 5156 may actsimilarly to the one or more ribs 5150 and/or the exoskeleton 5152disclosed above. In other words, the conductive portion 5156 may providea particular rigidity characteristic, e.g., providing rigidity onedirection while allowing for complete conformability in a seconddirection. In addition, it is contemplated that the conductive portion5156 may provide no additional rigidity to the reservoir 5110. Inparticular, the conductive portion 5156 would have the same flexibilityas the rest of the main body 5122 of the reservoir 5110. Such anarrangement would not include a metal conductive plate.

It is also contemplated that the entire reservoir 5110 may be made ofthermally conductive material (or material with low thermal impedance)such as, for example, polyethylene or some other thermally conductiveplastic. In this arrangement, the base unit heating element (not shown)may be positioned to thermally engage multiple walls of the reservoir5110 such that heat from the base unit heating element (not shown) maybe conveyed through more than one surface of the reservoir 5110.

The thickness of exterior walls of the reservoir 5110 may be sized tofacilitate the transfer of heat from the humidifier base heater (notshown) to liquid inside the reservoir 5110. For example, the walls maybe within a range of about 0.1 mm to about 1 mm. The thickness of thewalls may be 0.25 mm, 0.5 mm or 0.75 mm. In addition, the thickness ofthe walls of the reservoir 5110 may vary throughout the reservoir 5110as long as the walls are thin enough to allow sufficient transfer ofheat to maintain the liquid at a desired temperature.

A reservoir 5110 may comprise a set of conductive portions made ofthermally conductive material. The set of conductive portions could beused with a humidifier base 5006 with multiple heater surfaces orportions (as opposed to an exemplary humidifier base 5006 in which theheater only comprises a single heater portion located on a bottomsurface of the humidifier base 5006), such that each of the set ofconductive portions may engage with a heater surface or portion. In someforms, a humidifier base 5006 may comprise multiple heater surfaces orportions, all of which may engage with one continuous wall of thereservoir 5110 in use.

As discussed previously, the reservoir 5110 may expand upon the additionof water and/or pressurized gas. The expansion of the reservoir 5110 maycause the walls of the reservoir 5110 to engage the walls of thehumidifier base 5006. Thus, the expansion of the reservoir 5110 maycause (or improve) thermal engagement between the reservoir 5110 and aheater element (or elements) of the humidifier base 5006.

It is further contemplated that one or more heaters 5158 may be moldedat least partially within the walls 5160 of the reservoir 5110 (as shownin FIG. 5T) or secured to an interior surface of the reservoir 5110. Inaddition, a flexible tape heater 5162 may extend from the air inlet 5118through the interior of the reservoir 5110 and through the air outlet5120. It should be noted that the flexible tape heater 5162 may onlyextend a fraction of the length shown in FIG. 5U (e.g., the flexibletape heater 5162 may terminate before reaching the air outlet 5120).Also, a floating heater 5164 may be provided. The floating heater 5164may be configured to float on the liquid within the reservoir 5110.Electrical connections (not shown) for the heater could be provided onthe humidifier base 5006 by way of a plug and socket or other type ofconnection.

4.6.2.4 Water Level Indicator

The humidifier reservoir 5110 may comprise a water level indicator 5166as shown in FIG. 5D-5E. In some forms, the water level indicator 5166may provide one or more indications to a user such as the patient 1000or a care giver regarding a quantity of the volume of water in thehumidifier reservoir 5110. The one or more indications provided by thewater level indicator 5166 may include an indication of a maximum,predetermined volume of water, any portions thereof, such as 25%, 50% or75% or volumes such as 200 ml, 300 ml or 400 ml.

4.6.3 Humidifier Electrical & Thermal Components

The humidifier 5000 may comprise a number of electrical and/or thermalcomponents such as those listed below.

The reservoir 5110 may comprise an electrical circuit. In one form, thecircuit may comprise a substrate that also forms a part of a reservoirwall. The substrate may comprise a flexible polymer film, for examplefilm made from polyester, polyimide, polycarbonate, or polypropylene.Additionally, or alternatively, the substrate may be rigidly configured,such as a metal plate constructed from aluminium or a polymer such aspolycarbonate or polypropylene.

The electrical circuit may also comprise conductive ink printed onto thesubstrate to form electrical track(s). The electrical circuit mayfurther comprise one or more humidifier transducers 5116, which may besurface mounted onto a reservoir wall or otherwise adhered. Theelectrical circuit may comprise electrically resistive tracks, such as aheating circuit, as will be described in further detail below.

Thus, a wall of the reservoir 5110 (or a part thereof) may form asubstrate for a heat generating component such as an electricallyresistive heating track and/or for mounting one or more electricalcomponents such as a transducer. Electrical tracks and/or components maybe printed, adhered onto, surface mounted, or otherwise coupled with thesubstrate to create one or more electrical circuits on the reservoir5110. The one or more electrical circuits may be then electricallyconnectable to a power supply, such as the humidifier base 5006 or theRPT device 4000.

The reservoir 5110 may thus comprise one or more electrical connectors,each comprising one or more terminals for a power and/or electricalsignals (e.g. from a sensor). The one or more electrical connectors mayuse a wall of the reservoir 5110 as a substrate or comprise anadditional component connected thereto, coupled to the heater and/orsensor using any of various known means.

An RPT device 4000 and/or a humidifier base 5006 may thus comprise oneor more complementary connectors to couple to and/or receive the one ormore connectors of the reservoir 5110.

4.6.3.1 Humidifier Transducer(s)

The humidifier 5000 may comprise one or more humidifier transducers(sensors) 5116 instead of, or in addition to, transducers 4270 describedabove. Humidifier transducers 5116 may include one or more of an airpressure sensor 5168, an air flow rate transducer 5170, a temperaturesensor 5172, or a humidity sensor 5174 as shown in FIG. 5D. A humidifiertransducer 5174 may produce one or more output signals which may becommunicated to a controller such as the central controller 4230 and/ora humidifier controller 5176. In some forms, a humidifier transducer maybe located externally to the humidifier 5000 (such as in the air circuit4170) while communicating the output signal to the controller.

The reservoir 5110 may comprise one or more of the humidifiertransducers 5116. One or more transducers may be mounted directly ontothe reservoir 5110, such as by using a wall of the reservoir 5110 as asubstrate onto which an electrical circuit may be printed, adhered to orotherwise located.

4.6.3.1.1 Pressure Transducer

One or more pressure transducers 5168 may be provided to the humidifier5000 in addition to, or instead of, a pressure sensor 4272 provided inthe RPT device 4000.

4.6.3.1.2 Flow Rate Transducer

One or more flow rate transducers 5170 may be provided to the humidifier5000 in addition to, or instead of, a flow rate sensor 4274 provided inthe RPT device 4000.

4.6.3.1.3 Temperature Transducer

The humidifier 5000 may comprise one or more temperature transducers5172. The one or more temperature transducers 5172 may be configured tomeasure one or more temperatures such as of the heater 5158 and/or ofthe flow of air downstream of the humidifier outlet 5004. In some forms,the humidifier 5000 may further comprise a temperature sensor 5172 todetect the temperature of the ambient air.

4.6.3.1.4 Humidity Transducer

In one form, the humidifier 5000 may comprise one or more humiditysensors 5174 to detect a humidity of a gas, such as the ambient air. Thehumidity sensor 5174 may be placed towards the humidifier outlet 5004 insome forms to measure a humidity of the gas delivered from thehumidifier 5000. The humidity sensor may be an absolute humidity sensoror a relative humidity sensor.

4.6.3.2 Heating Element

As discussed above, a heating element (or a heater) may be provided tothe humidifier 5000 in some cases to provide a heat input to one or moreof the volume of water in the humidifier reservoir 5110 and/or to theflow of air. The heating element may comprise a heat generatingcomponent such as an electrically resistive heating track. One suitableexample of a heating element is a layered heating element such as onedescribed in the PCT Patent Application Publication No. WO 2012/171072,which is incorporated herewith by reference in its entirety.

In some forms, the heating element may be provided in the humidifierbase 5006 where heat may be provided to the humidifier reservoir 5110primarily by conduction.

The humidifier 5000 may comprise one or more heaters or heating regionsin the at least one wall defining the receiving space 5112. Acorresponding humidifier reservoir 5110 may be configured such that inuse, the one or more heating regions may effectively transfer heat tothe reservoir 5110, such as by being engaged thereto.

The heating regions may be disposed within the receiving space 5112. Inone example, the at least one wall defining the receiving space 5112 maycomprise a bottom wall and four, orthogonal side walls, thus defining arectangular prism shaped receiving space. In such an arrangement, aheating region may be disposed on the bottom wall of the receiving space5112. Additionally, or alternatively, heating regions may be disposed inone or more of each side wall defining the receiving space 5112.Furthermore, it will be understood that a single wall may comprise aplurality of heating regions, such as a first heating region above asecond heating region. In such a configuration they may be separatelycontrolled.

In some forms, the reservoir 5110 may comprise a heater configured toheat the volume of water contained therein. The reservoir 5110 maycomprise one or more heating regions, such as one, two, three, four,five, ten, fifteen or twenty for example, although any other numbers maybe suitable. The heating regions may be distributed throughout thereservoir 5110 in some forms such as evenly distributed throughout thereservoir 5110.

Additionally, or alternatively, the heating regions may be distributedthroughout the reservoir 5110 such that when in use, a set of heatingregions may be disposed towards a bottom wall of the receiving space5112, and a set of heating regions may be disposed towards one or moreof each side wall defining the receiving space 5112.

The reservoir 5110 may comprise a set of heating regions configured tocontrol a temperature at a point of high temperature gradients, such asat an interface between air in the reservoir 5110 and ambient air. Forexample, the reservoir 5110 may comprise a set of heating regionsdisposed where the reservoir 5110 may be exposed to the ambient air,such as a top surface (away from the frame 5154) of the reservoir 5110in a configuration shown in FIG. 5Q.

In one aspect, such interface heating regions may reduce a temperaturedistribution within the reservoir 5110. Thus, placement of a set ofheating regions at an interface between ambient air and air in thereservoir 5110 may advantageously an accurate control of air temperaturewithin the reservoir 5110.

Each of the heating regions may be separately controlled, as describedabove for example. In some forms, the reservoir 5110 may comprise afirst set of heating regions configured to heat a first chamber 5142 anda second set of heating regions configured to heat a second chamber5144. The first chamber 5142 and the second chamber 5144 may beseparated by a backflow prevention system, such as a divider 5140 asshown in FIG. 5L.

Thus, the first set of heating regions may be configured tosubstantially heat a flow of air in the first chamber 5142 prior to itentering the second chamber 5144, and the second set of heating regionsmay be configured to heat air flowing through the second chamber 5144 aswell as the volume of water contained therein. A potential advantage ofsuch an arrangement may be that the saturation point of the air flow maybe increased, allowing the air flow to advantageously contain a highermoisture content therein.

In one form, the first set of heating regions may be configured todeliver an increased power output when a temperature of the volume ofwater in the reservoir 5110 is low. The increased power output maythereby further pre-heat the air flow before it comes into contact withthe volume of water and/or the water vapour (e.g. in the secondchamber). One suitable exemplary scenario may be during a start-upphase, where the humidifier 5000 and/or the RPT device 4000 has beenactivated or switched on recently, and the volume of water has notsufficiently warmed up. Another example may be when an ambienttemperature is particularly low, wherein pre-heating the air flow may bebeneficial.

Heating requirements for air and water may be different for a number ofreasons. For example, the volume of water in a reservoir 5110 is astationary (or at least slowly changing), fixed, quantity while airflows through the humidifier 5000, at a flow rate of up to approximately100 L/min. However, the heat capacity of air is lower (approximately ¼)than that of water, and the density of air is approximately 1/1000^(th)of that of water. It may therefore require substantially less energy toheat air than it does to heat water. The first set of heating regionsmay be thus configured to deliver a substantially lower heat outputquantity than the second set of heating regions, such as two, five, ten,twenty times lower, while meeting heating requirements for both the airflow as well as the volume of water.

4.6.3.3 Humidifier Controller

According to one arrangement of the present technology, a humidifier5000 may comprise a humidifier controller 5176 as shown in FIG. 5A. Inone form, the humidifier controller 5176 may be a part of the centralcontroller 4230. In another form, the humidifier controller 5176 may bea separate controller, which may be in communication with the centralcontroller 4230.

In one form, the humidifier controller 5176 may receive as inputsmeasures of characteristics (such as temperature, humidity, pressureand/or flow rate), for example of the flow of air, the water in thereservoir 5110 and/or the humidifier 5000. The humidifier controller5176 may also be configured to execute or implement humidifieralgorithms and/or deliver one or more output signals.

As shown in FIG. 5A, the humidifier controller 5176 may comprise one ormore controllers, such as a central humidifier controller 5178, a heatedair circuit controller 5180 configured to control the temperature of aheated air circuit 4170 and/or a heating element controller 5182configured to control the temperature of the base unit heater (notshown).

4.7 GLOSSARY

For the purposes of the present technology disclosure, in certain formsof the present technology, one or more of the following definitions mayapply. In other forms of the present technology, alternative definitionsmay apply.

4.7.1 General

Air: In certain forms of the present technology, air may be taken tomean atmospheric air, and in other forms of the present technology airmay be taken to mean some other combination of breathable gases, e.g.atmospheric air enriched with oxygen.

Ambient: In certain forms of the present technology, the term ambientwill be taken to mean (i) external of the treatment system or patient,and (ii) immediately surrounding the treatment system or patient.

For example, ambient humidity with respect to a humidifier may be thehumidity of air immediately surrounding the humidifier, e.g. thehumidity in the room where a patient is sleeping. Such ambient humiditymay be different to the humidity outside the room where a patient issleeping.

In another example, ambient pressure may be the pressure immediatelysurrounding or external to the body.

In certain forms, ambient (e.g., acoustic) noise may be considered to bethe background noise level in the room where a patient is located, otherthan for example, noise generated by an RPT device or emanating from amask or patient interface. Ambient noise may be generated by sourcesoutside the room.

Respiratory Pressure Therapy (RPT): The application of a supply of airto an entrance to the airways at a treatment pressure that is typicallypositive with respect to atmosphere.

Continuous Positive Airway Pressure (CPAP) therapy: Respiratory pressuretherapy in which the treatment pressure is approximately constantthrough a respiratory cycle of a patient. In some forms, the pressure atthe entrance to the airways will be slightly higher during exhalation,and slightly lower during inhalation. In some forms, the pressure willvary between different respiratory cycles of the patient, for example,being increased in response to detection of indications of partial upperairway obstruction, and decreased in the absence of indications ofpartial upper airway obstruction.

Patient: A person, whether or not they are suffering from a respiratorydisease.

Automatic Positive Airway Pressure (APAP) therapy: CPAP therapy in whichthe treatment pressure is automatically adjustable, e.g. from breath tobreath, between minimum and maximum limits, depending on the presence orabsence of indications of SDB events.

4.7.2 RPT Device Parameters

Flow rate: The instantaneous volume (or mass) of air delivered per unittime. While flow rate and ventilation have the same dimensions of volumeor mass per unit time, flow rate is measured over a much shorter periodof time. In some cases, a reference to flow rate will be a reference toa scalar quantity, namely a quantity having magnitude only. In othercases, a reference to flow rate will be a reference to a vectorquantity, namely a quantity having both magnitude and direction.

Leak: The word leak will be taken to be an unintended flow of air. Inone example, leak may occur as the result of an incomplete seal betweena mask and a patient's face. In another example leak may occur in aswivel elbow to the ambient.

Pressure: Force per unit area. Pressure may be measured in a range ofunits, including cmH₂O, g-f/cm², hectopascal. 1 cmH₂O is equal to 1g-f/cm² and is approximately 0.98 hectopascal. In this specification,unless otherwise stated, pressure is given in units of cmH₂O.

4.8 OTHER REMARKS

A portion of the disclosure of this patent document contains materialwhich is subject to copyright protection. The copyright owner has noobjection to the facsimile reproduction by anyone of the patent documentor the patent disclosure, as it appears in Patent Office patent files orrecords, but otherwise reserves all copyright rights whatsoever.

Unless the context clearly dictates otherwise and where a range ofvalues is provided, it is understood that each intervening value, to thetenth of the unit of the lower limit, between the upper and lower limitof that range, and any other stated or intervening value in that statedrange is encompassed within the technology. The upper and lower limitsof these intervening ranges, which may be independently included in theintervening ranges, are also encompassed within the technology, subjectto any specifically excluded limit in the stated range. Where the statedrange includes one or both of the limits, ranges excluding either orboth of those included limits are also included in the technology.

Furthermore, where a value or values are stated herein as beingimplemented as part of the technology, it is understood that such valuesmay be approximated, unless otherwise stated, and such values may beutilized to any suitable significant digit to the extent that apractical technical implementation may permit or require it.

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which this technology belongs. Although any methods andmaterials similar or equivalent to those described herein can also beused in the practice or testing of the present technology, a limitednumber of the exemplary methods and materials are described herein.

When a particular material is identified as being used to construct acomponent, obvious alternative materials with similar properties may beused as a substitute. Furthermore, unless specified to the contrary, anyand all components herein described are understood to be capable ofbeing manufactured and, as such, may be manufactured together orseparately.

It must be noted that as used herein and in the appended claims, thesingular forms “a”, “an”, and “the” include their plural equivalents,unless the context clearly dictates otherwise.

All publications mentioned herein are incorporated herein by referencein their entirety to disclose and describe the methods and/or materialswhich are the subject of those publications. The publications discussedherein are provided solely for their disclosure prior to the filing dateof the present application. Nothing herein is to be construed as anadmission that the present technology is not entitled to antedate suchpublication by virtue of prior invention. Further, the dates ofpublication provided may be different from the actual publication dates,which may need to be independently confirmed.

The terms “comprises” and “comprising” should be interpreted asreferring to elements, components, or steps in a non-exclusive manner,indicating that the referenced elements, components, or steps may bepresent, or utilized, or combined with other elements, components, orsteps that are not expressly referenced.

The subject headings used in the detailed description are included onlyfor the ease of reference of the reader and should not be used to limitthe subject matter found throughout the disclosure or the claims. Thesubject headings should not be used in construing the scope of theclaims or the claim limitations.

Although the technology herein has been described with reference toparticular examples, it is to be understood that these examples aremerely illustrative of the principles and applications of thetechnology. In some instances, the terminology and symbols may implyspecific details that are not required to practice the technology. Forexample, although the terms “first” and “second” may be used, unlessotherwise specified, they are not intended to indicate any order but maybe utilised to distinguish between distinct elements. Furthermore,although process steps in the methodologies may be described orillustrated in an order, such an ordering is not required. Those skilledin the art will recognize that such ordering may be modified and/oraspects thereof may be conducted concurrently or even synchronously.

It is therefore to be understood that numerous modifications may be madeto the illustrative examples and that other arrangements may be devisedwithout departing from the spirit and scope of the technology.

4.9 REFERENCE SIGNS LIST

-   1000 patient-   1100 bed partner-   3000 patient interface-   3100 seal-forming structure-   3200 plenum chamber-   3300 stabilising structure-   3400 vent-   3600 connection port-   3700 forehead support-   4000 RPT device-   4010 external housing-   4012 upper portion-   4014 lower portion-   4015 panel-   4016 chassis-   4018 handle-   4020 pneumatic block-   4100 mechanical and pneumatic components-   4110 air filter-   4112 inlet air filter-   4114 outlet air filter-   4122 inlet muffler-   4124 outlet muffler-   4140 pressure generator-   4142 blower-   4144 motor-   4160 anti-spill back valve-   4170 air circuit-   4180 supplemental oxygen-   4200 electrical components-   4202 printed circuit board assembly-   4210 power supply-   4220 input device-   4230 central controller-   4232 clock-   4240 therapy device controller-   4250 protection circuit-   4260 memory-   4270 transducer-   4272 pressure sensor-   4274 flow rate sensor-   4276 motor speed transducer-   4280 data communication interface-   4282 remote external communication network-   4284 local external communication network-   4286 remote external device-   4288 local external device-   4290 output device-   4292 display driver-   4294 display-   5000 humidifier-   5002 humidifier inlet-   5004 humidifier outlet-   5006 humidifier base-   5110 reservoir-   5112 receiving space-   5114 engaging portion-   5116 humidifier transducer or sensor-   5118 air inlet-   5120 air outlet-   5122 main body-   5124 connector-   5126 connector-   5128 top portion-   5130 bottom portion-   5132 securing mechanism-   5134 seal-   5136 port-   5138 opening-   5140 divider-   5142 first chamber-   5144 second chamber-   5146 opening-   5148 check valve-   5150 rib-   5152 exoskeleton-   5154 frame-   5156 conductive portion-   5158 heater-   5160 wall-   5162 flexible tape heater-   5164 floating heater-   5166 water level indicator-   5167 travel bag-   5168 first receptacle-   5170 second receptacle-   5172 securement strap-   5174 third receptacle-   5175 securement strap-   5176 humidifier controller-   5178 central humidifier controller-   5180 heated air circuit controller-   5182 heating element controller

1. A humidifier for humidifying a flow of air to be delivered to apatient, the humidifier comprising: a base unit comprising at least onewall defining a receiving space; a variable volume reservoir configuredto hold a body of water and receive the flow of air to humidify the flowof air for delivery to the patient; and a heater for heating the body ofwater, wherein the receiving space is configured to receive the variablevolume reservoir and the variable volume reservoir is conformable to ashape of the receiving space.
 2. The humidifier of claim 1, wherein thevariable volume reservoir is collapsible to a flat plate.
 3. Thehumidifier of claim 1, wherein the at least one wall defines a prismshaped receiving space.
 4. The humidifier of claim 1, wherein thevariable volume reservoir comprises low thermal impedance materialconfigured to engage the heater in use.
 5. The humidifier of claim 4,wherein the low thermal impedance material comprises at least one ofpolyethylene or polyamide.
 6. The humidifier of claim 1, wherein thevariable volume reservoir does not comprise a metal plate.
 7. Thehumidifier of claim 1, wherein the variable volume reservoir comprisesthe heater.
 8. The humidifier of claim 7, wherein the heater is aflexible tape heater.
 9. The humidifier of claim 8, wherein at least apart of the heater is molded within a wall of the variable volumereservoir.
 10. The humidifier of claim 1, wherein the variable volumereservoir comprises an air inlet and a water inlet.
 11. The humidifierof claim 10, wherein the air inlet comprises an ISO standard connectorfor fluidly connecting to a respiratory apparatus.
 12. A humidifier foruse with a respiratory pressure therapy (RPT) apparatus, the humidifiercomprising: a flexible chamber configured to hold a body of water andreceive a flow of air from the RPT apparatus to humidify the flow ofair; and a base unit configured to support the flexible chamber, theflexible chamber being configured to conform to a shape of a receivingspace of the base unit in use.
 13. The humidifier of claim 12, whereinthe flexible chamber is configured to expand during use.
 14. Thehumidifier of claim 12, wherein the flexible chamber comprises aflexible main body.
 15. The humidifier of claim 12, wherein the flexiblechamber comprises a rigidizing structure for the flexible main body. 16.The humidifier of claim 15, wherein the rigidizing structure is one ormore ribs extending along an interior surface of the flexible main body.17. The humidifier of claim 15, wherein the rigidizing structure is anexoskeleton extending across an outer surface of the flexible main body.18. The humidifier of claim 12, wherein the base unit comprises aheating element.
 19. The humidifier of claim 17, wherein the heatingelement comprises a plurality of heating regions.
 20. The humidifier ofclaim 19, wherein the flexible chamber is configured to engage each ofthe plurality of heating regions in use.
 21. A humidifier for acontinuous positive airway pressure (CPAP) apparatus, the humidifiercomprising: a conformable chamber configured to hold a body of water andreceive a flow of gas from the CPAP apparatus to humidify the flow ofgas; and at least one wall defining a receiving space configured toretain the flexible chamber in a fixed position relative to the CPAPapparatus, wherein the at least one wall of the receiving space isconfigured to force the conformable chamber into a predetermined shapeupon the conformable chamber being received by the receiving space. 22.The humidifier of claim 21, wherein the receiving space comprises aheating element configured to engage at least one of the walls of theconformable chamber when the conformable chamber is received by thereceiving space.
 23. The humidifier of claim 21, wherein the conformablechamber comprises a heating element.
 24. The humidifier of claim 21,wherein the conformable chamber comprises an air inlet with a checkvalve.
 25. The humidifier of claim 24, wherein the check valve isconfigured to open during a treatment session of the CPAP apparatus. 26.The humidifier of claim 21, wherein the conformable chamber comprises adivider that divides the conformable chamber into two subchambers. 27.The humidifier of claim 26, wherein the divider is configured to preventliquid from flowing through an air inlet of the conformable chamber whenthe conformable chamber is tilted from an operating configuration. 28.The humidifier of claim 21, wherein the conformable chamber comprises arigidizing structure to add rigidity to the conformable chamber.
 29. Thehumidifier of claim 28, wherein the rigidizing structure is positionedinside the conformable chamber.
 30. The humidifier of claim 28, whereinthe rigidizing structure is positioned on an outside surface of theconformable chamber.
 31. The humidifier of claim 21, wherein theconformable chamber is pre-filled with water.
 32. A humidifier for acontinuous positive airway pressure (CPAP) apparatus, the humidifiercomprising: a flexible chamber configured to hold a body of water andreceive pressurized gas from the CPAP apparatus to humidify thepressurized gas, the flexible chamber comprises a rigidizer configuredto prevent the flexible chamber from collapsing in on itself, whereinthe flexible chamber is configured to directly couple to the CPAPapparatus.
 33. The humidifier of claim 31, wherein the rigidizer is atleast one of a rib structure positioned inside the flexible chamber andan exoskeleton structure positioned outside the flexible chamber.